Home NDC 63029-668 GOODYS
Product NDC 63029-668
11-digit product format 630290668
Labeler code 63029
Product ID 63029-668_7d78e8c1-f247-413e-aa4b-c07d1ef583d0
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen, Aspirin, and Caffeine
Dosage form POWDER
Route ORAL
Labeler Medtech Products Inc.
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-02-02
Substance ACETAMINOPHEN; ASPIRIN; CAFFEINE
Active strength 500; 500; 130 mg/1; mg/1; mg/1
Pharmacologic classes Anti-Inflammatory Agents, Non-Steroidal [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Methylxanthine [EPC], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC], Xanthines [CS]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base GOODYS
Brand name suffix MAX
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 500 mg/1 ASPIRIN 500 mg/1 CAFFEINE 130 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 362O9ITL9D Internal UNII lookup R16CO5Y76E Internal UNII lookup 3G6A5W338E Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2734143 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63029-668-16 GOODYSMAX 16 in 1 CARTON POWDER 16 1
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 79 · 1,579 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 63029-668-16 63029066816 16 POWDER in 1 CARTON (63029-668-16) 16 powder 2026-02-02 No No Current